136609-53-5 Usage
Molecular structure
2-[(5-(3,5-dimethylpyrazol-1-yl)pent-1-yl)sulphinyl]-4,5-diphenylimidazole has a complex molecular structure that includes a sulphinyl group, two phenyl groups, an imidazole ring, a pentyl chain, and a pyrazol-1-yl substituent.
Sulphinyl group
The compound contains a sulphinyl group (R2S), which is a functional group consisting of a sulfur atom bonded to two organic groups. This group imparts specific chemical reactivity and properties to the molecule.
Phenyl groups
Two phenyl groups (C6H5) are attached to the imidazole ring, which is a heterocyclic aromatic ring system. The presence of these groups contributes to the compound's stability and potential applications in various fields.
Imidazole ring
The core structure of the compound is an imidazole ring, a five-membered heterocyclic ring containing one nitrogen atom and four carbon atoms. This ring is known for its aromaticity and is a common structural motif in many biologically active compounds.
Pentyl chain
A pentyl chain (C5H11) is attached to the imidazole ring, which is a five-carbon alkyl chain. This chain may influence the compound's solubility, lipophilicity, and other physical properties.
Pyrazol-1-yl substituent
The pentyl chain features a 3,5-dimethylpyrazol-1-yl substituent, which is a bicyclic ring system with two nitrogen atoms. This substituent may contribute to the compound's biological activity and potential applications in pharmaceuticals.
Potential applications
2-[(5-(3,5-dimethylpyrazol-1-yl)pent-1-yl)sulphinyl]-4,5-diphenylimidazole may have potential applications in pharmaceuticals or materials science due to its diverse functional groups and potential for unique biochemical or physical properties.
Further research
To fully understand the potential uses and properties of this chemical, additional research is needed to explore its reactivity, stability, and interactions with biological systems.
Check Digit Verification of cas no
The CAS Registry Mumber 136609-53-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,6,0 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 136609-53:
(8*1)+(7*3)+(6*6)+(5*6)+(4*0)+(3*9)+(2*5)+(1*3)=135
135 % 10 = 5
So 136609-53-5 is a valid CAS Registry Number.
136609-53-5Relevant academic research and scientific papers
PROCESS FOR SYNTHESIS OF SUBSTITUTED SULPHOXIDES
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, (2008/06/13)
A novel process for enantioselective synthesis of single enantiomers of omeprazole or its alkaline salts, of other optically pure substituted 2-(2-pyridinylmethyl-sulphinyl) -1H-benzimidazoles as well as of other structurally related sulphoxides or their alkaline salts. The claimed process is an asymmetric oxidation of a pro-chiral sulphide to the single enantiomers or an enantiomerically enriched form of the corresponding sulphoxide. The application also claims the enantiomeric sulphoxide products produced by the process and their use in medicine
LARGE SCALE ASYMMETRIC SYNTHESIS OF A BIOLOGICALLY ACTIVE SULFOXIDE
Pitchen, Philippe,France, Christopher J.,McFarlane, Ian M.,Newton, Christopher G.,Thompson, David M.
, p. 485 - 488 (2007/10/02)
The asymmetric synthesis of sulfoxide RP 73163 is described.The synthesis strategy is based on the enantioselective oxidation of a suitablay designed prochiral methyl sulfide, followed by a alkylation of the resulting sulfoxide.Keywords: Asymmetric sulfoi
Imidazoles as ACAT inhibitor
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, (2008/06/13)
The enantiomer of 2-[5-(3,5-dimethylpyrazol-1-yl)pentylsulphinyl]-4,5-diphenylimidazole which, in dilute solution in dichloromethane at room temperature, rotates plane-polarised light of the sodium D wavelength to the right, or a pharmaceutically acceptab
